Loss of Neuroprotective Factors in Neurodegenerative Dementias: The End or the Starting Point?

被引:28
作者
Benussi, Luisa [1 ]
Binetti, Giuliano [1 ,2 ]
Ghidoni, Roberta [1 ]
机构
[1] IRCCS Ist Ctr San Giovanni Dio Fatebenefratelli, Mol Markers Lab, Brescia, Italy
[2] IRCCS Ist Ctr San Giovanni Dio Fatebenefratelli, MAC Memory Ctr, Brescia, Italy
关键词
BDNF; progranulin; cystatin C; biomarkers; frontotemporal dementia; Alzheimer's disease; Lewy body dementia; FRONTOTEMPORAL LOBAR DEGENERATION; ACTIVITY-DEPENDENT SECRETION; CYSTATIN-C VARIANT; BDNF MESSENGER-RNA; ALZHEIMERS-DISEASE; NEUROTROPHIC-FACTOR; AMYLOID-BETA; CEREBROSPINAL-FLUID; GENE-EXPRESSION; PROGRANULIN DEFICIENCY;
D O I
10.3389/fnins.2017.00672
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent clinical, genetic and biochemical experimental evidences highlight the existence of common molecular pathways underlying neurodegenerative diseases. In this review, we will explore a key common pathological mechanism, i.e., the loss of neuroprotective factors, across the three major neurodegenerative diseases leading to dementia: Alzheimer's disease (AD), Frontotemporal dementia (FTD) and Lewy body dementia (LBD). We will report evidences that the Brain Derived Neurotrophic Factor (BDNF), the most investigated and characterized brain neurotrophin, progranulin, a multi-functional adipokine with trophic and growth factor properties, and cystatin C, a neuroprotective growth factor, are reduced in AD, FTD, and LBD. Moreover, we will review the molecular mechanism underlying the loss of neuroprotective factors in neurodegenerative diseases leading to dementia, with a special focus on endo-lysosomal pathway and intercellular communication mediated by extracellular vesicles. Exploring the shared commonality of disease mechanisms is of pivotal importance to identify novel potential therapeutic targets and to develop treatments to delay, slow or block disease progression.
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页数:8
相关论文
共 107 条
[1]   GRN Thr272fs Clinical Heterogeneity: A Case with Atypical Late Onset Presenting with a Dementia with Lewy Bodies Phenotype [J].
Arosio, Beatrice ;
Abbate, Carlo ;
Galimberti, Daniela ;
Rossi, Paolo Dionigi ;
Inglese, Silvia ;
Fenoglio, Chiara ;
Ridolfi, Elisa ;
Gussago, Cristina ;
Casati, Martina ;
Tedone, Enzo ;
Ferri, Evelyn ;
Serpente, Maria ;
Scarpini, Elio ;
Mari, Daniela .
JOURNAL OF ALZHEIMERS DISEASE, 2013, 35 (04) :669-674
[2]   Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 [J].
Baker, Matt ;
Mackenzie, Ian R. ;
Pickering-Brown, Stuart M. ;
Gass, Jennifer ;
Rademakers, Rosa ;
Lindholm, Caroline ;
Snowden, Julie ;
Adamson, Jennifer ;
Sadovnick, A. Dessa ;
Rollinson, Sara ;
Cannon, Ashley ;
Dwosh, Emily ;
Neary, David ;
Melquist, Stacey ;
Richardson, Anna ;
Dickson, Dennis ;
Berger, Zdenek ;
Eriksen, Jason ;
Robinson, Todd ;
Zehr, Cynthia ;
Dickey, Chad A. ;
Crook, Richard ;
McGowan, Eileen ;
Mann, David ;
Boeve, Bradley ;
Feldman, Howard ;
Hutton, Mike .
NATURE, 2006, 442 (7105) :916-919
[3]   Granulins: the structure and function of an emerging family of growth factors [J].
Bateman, A ;
Bennett, HPJ .
JOURNAL OF ENDOCRINOLOGY, 1998, 158 (02) :145-151
[4]   Increased pro-nerve growth factor and decreased brain-derived neurotrophic factor in non-Alzheimer's disease tauopathies [J].
Belrose, Jillian C. ;
Masoudi, Raheleh ;
Michalski, Bernadeta ;
Fahnestock, Margaret .
NEUROBIOLOGY OF AGING, 2014, 35 (04) :926-933
[5]   Alzheimer disease-associated cystatin C variant undergoes impaired secretion [J].
Benussi, L ;
Ghidoni, R ;
Steinhoff, T ;
Alberici, AA ;
Villa, A ;
Mazzoli, F ;
Nicosia, F ;
Barbiero, L ;
Broglio, L ;
Feudatari, E ;
Signorini, S ;
Finckh, U ;
Nitsch, RM ;
Binetti, G .
NEUROBIOLOGY OF DISEASE, 2003, 13 (01) :15-21
[6]   The CST3 B haplotype is associated with frontotemporal lobar degeneration [J].
Benussi, L. ;
Ghidoni, R. ;
Galimberti, D. ;
Boccardi, M. ;
Fenoglio, C. ;
Scarpini, E. ;
Frisoni, G. B. ;
Binetti, G. .
EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 (01) :143-146
[7]  
BENUSSI L, 2006, HUMAN STEFINS CYSTAT, P115
[8]   Loss of exosomes in progranulin-associated frontotemporal dementia [J].
Benussi, Luisa ;
Ciani, Miriam ;
Tonoli, Elisa ;
Morbin, Michela ;
Palamara, Luisa ;
Albani, Diego ;
Fusco, Federica ;
Forloni, Gianluigi ;
Glionna, Michela ;
Baco, Monika ;
Paterlini, Anna ;
Fostinelli, Silvia ;
Santini, Benedetta ;
Galbiati, Elisabetta ;
Gagni, Paola ;
Cretich, Marina ;
Binetti, Giuliano ;
Tagliavini, Fabrizio ;
Prosperi, Davide ;
Chiari, Marcella ;
Ghidoni, Roberta .
NEUROBIOLOGY OF AGING, 2016, 40 :41-49
[9]   Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide [J].
Benussi, Luisa ;
Ghidoni, Roberta ;
Pegoiani, Eleonora ;
Moretti, Davide V. ;
Zanetti, Orazio ;
Binetti, Giuliano .
NEUROBIOLOGY OF DISEASE, 2009, 33 (03) :379-385
[10]   Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database [J].
Bertram, Lars ;
McQueen, Matthew B. ;
Mullin, Kristina ;
Blacker, Deborah ;
Tanzi, Rudolph E. .
NATURE GENETICS, 2007, 39 (01) :17-23